Imaging mass cytometry reveals the prominent role of myeloid cells at the maternal-fetal interface

Although the immunological complexity of the maternal-fetal interface is well appreciated, the actual interaction of maternal immune cells and fetal trophoblasts is insufficiently understood. To comprehend the composition and spatial orientation of maternal immune cells and fetal extravillous tropho...

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Veröffentlicht in:iScience Jg. 25; H. 7; S. 104648
Hauptverfasser: Krop, Juliette, van der Zwan, Anita, Ijsselsteijn, Marieke E., Kapsenberg, Hanneke, Luk, Sietse J., Hendriks, Sanne H., van der Keur, Carin, Verleng, Lotte J., Somarakis, Antonis, van der Meeren, Lotte, Haasnoot, Geert, Bos, Manon, de Miranda, Noel F.C.C., Chuva de Sousa Lopes, Susana M., van der Hoorn, Marie-Louise P., Koning, Frits, Claas, Frans H.J., Heidt, Sebastiaan, Eikmans, Michael
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Sprache:Englisch
Veröffentlicht: Elsevier Inc 15.07.2022
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ISSN:2589-0042, 2589-0042
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Abstract Although the immunological complexity of the maternal-fetal interface is well appreciated, the actual interaction of maternal immune cells and fetal trophoblasts is insufficiently understood. To comprehend the composition and spatial orientation of maternal immune cells and fetal extravillous trophoblasts, we applied imaging mass cytometry on decidua basalis of the three trimesters of healthy pregnancy. Within all trimesters, we observed considerably higher frequencies of myeloid cells in the decidua than is seen with single-cell suspension techniques. Moreover, they were the most pronounced cell type in the microenvironment of other decidual cells. In first trimester, HLA-DR- macrophages represented the most abundant myeloid subcluster and these cells were frequently observed in the vicinity of trophoblasts. At term, HLA-DR+ macrophage subclusters were abundantly present and frequently observed in the microenvironment of T cells. Taken together, our results highlight the dynamic role of myeloid cells at the human maternal-fetal interface throughout gestation. [Display omitted] •Frequency of myeloid cells is underestimated after tissue digestion•Myeloid cells could support NK cells with proper trophoblast invasion•Myeloid cells are dynamic in their role throughout gestation Biological sciences; Immunology; Biotechnology; Biological sciences research methodologies
AbstractList Although the immunological complexity of the maternal-fetal interface is well appreciated, the actual interaction of maternal immune cells and fetal trophoblasts is insufficiently understood. To comprehend the composition and spatial orientation of maternal immune cells and fetal extravillous trophoblasts, we applied imaging mass cytometry on decidua basalis of the three trimesters of healthy pregnancy. Within all trimesters, we observed considerably higher frequencies of myeloid cells in the decidua than is seen with single-cell suspension techniques. Moreover, they were the most pronounced cell type in the microenvironment of other decidual cells. In first trimester, HLA-DR- macrophages represented the most abundant myeloid subcluster and these cells were frequently observed in the vicinity of trophoblasts. At term, HLA-DR+ macrophage subclusters were abundantly present and frequently observed in the microenvironment of T cells. Taken together, our results highlight the dynamic role of myeloid cells at the human maternal-fetal interface throughout gestation.
Although the immunological complexity of the maternal-fetal interface is well appreciated, the actual interaction of maternal immune cells and fetal trophoblasts is insufficiently understood. To comprehend the composition and spatial orientation of maternal immune cells and fetal extravillous trophoblasts, we applied imaging mass cytometry on decidua basalis of the three trimesters of healthy pregnancy. Within all trimesters, we observed considerably higher frequencies of myeloid cells in the decidua than is seen with single-cell suspension techniques. Moreover, they were the most pronounced cell type in the microenvironment of other decidual cells. In first trimester, HLA-DR- macrophages represented the most abundant myeloid subcluster and these cells were frequently observed in the vicinity of trophoblasts. At term, HLA-DR+ macrophage subclusters were abundantly present and frequently observed in the microenvironment of T cells. Taken together, our results highlight the dynamic role of myeloid cells at the human maternal-fetal interface throughout gestation. • Frequency of myeloid cells is underestimated after tissue digestion • Myeloid cells could support NK cells with proper trophoblast invasion • Myeloid cells are dynamic in their role throughout gestation Biological sciences; Immunology; Biotechnology; Biological sciences research methodologies
Although the immunological complexity of the maternal-fetal interface is well appreciated, the actual interaction of maternal immune cells and fetal trophoblasts is insufficiently understood. To comprehend the composition and spatial orientation of maternal immune cells and fetal extravillous trophoblasts, we applied imaging mass cytometry on decidua basalis of the three trimesters of healthy pregnancy. Within all trimesters, we observed considerably higher frequencies of myeloid cells in the decidua than is seen with single-cell suspension techniques. Moreover, they were the most pronounced cell type in the microenvironment of other decidual cells. In first trimester, HLA-DR- macrophages represented the most abundant myeloid subcluster and these cells were frequently observed in the vicinity of trophoblasts. At term, HLA-DR+ macrophage subclusters were abundantly present and frequently observed in the microenvironment of T cells. Taken together, our results highlight the dynamic role of myeloid cells at the human maternal-fetal interface throughout gestation. [Display omitted] •Frequency of myeloid cells is underestimated after tissue digestion•Myeloid cells could support NK cells with proper trophoblast invasion•Myeloid cells are dynamic in their role throughout gestation Biological sciences; Immunology; Biotechnology; Biological sciences research methodologies
Although the immunological complexity of the maternal-fetal interface is well appreciated, the actual interaction of maternal immune cells and fetal trophoblasts is insufficiently understood. To comprehend the composition and spatial orientation of maternal immune cells and fetal extravillous trophoblasts, we applied imaging mass cytometry on decidua basalis of the three trimesters of healthy pregnancy. Within all trimesters, we observed considerably higher frequencies of myeloid cells in the decidua than is seen with single-cell suspension techniques. Moreover, they were the most pronounced cell type in the microenvironment of other decidual cells. In first trimester, HLA-DR- macrophages represented the most abundant myeloid subcluster and these cells were frequently observed in the vicinity of trophoblasts. At term, HLA-DR+ macrophage subclusters were abundantly present and frequently observed in the microenvironment of T cells. Taken together, our results highlight the dynamic role of myeloid cells at the human maternal-fetal interface throughout gestation.Although the immunological complexity of the maternal-fetal interface is well appreciated, the actual interaction of maternal immune cells and fetal trophoblasts is insufficiently understood. To comprehend the composition and spatial orientation of maternal immune cells and fetal extravillous trophoblasts, we applied imaging mass cytometry on decidua basalis of the three trimesters of healthy pregnancy. Within all trimesters, we observed considerably higher frequencies of myeloid cells in the decidua than is seen with single-cell suspension techniques. Moreover, they were the most pronounced cell type in the microenvironment of other decidual cells. In first trimester, HLA-DR- macrophages represented the most abundant myeloid subcluster and these cells were frequently observed in the vicinity of trophoblasts. At term, HLA-DR+ macrophage subclusters were abundantly present and frequently observed in the microenvironment of T cells. Taken together, our results highlight the dynamic role of myeloid cells at the human maternal-fetal interface throughout gestation.
ArticleNumber 104648
Author Verleng, Lotte J.
Kapsenberg, Hanneke
Krop, Juliette
van der Zwan, Anita
Eikmans, Michael
Bos, Manon
Heidt, Sebastiaan
van der Hoorn, Marie-Louise P.
Ijsselsteijn, Marieke E.
Haasnoot, Geert
Chuva de Sousa Lopes, Susana M.
van der Meeren, Lotte
de Miranda, Noel F.C.C.
Somarakis, Antonis
Luk, Sietse J.
Koning, Frits
Claas, Frans H.J.
Hendriks, Sanne H.
van der Keur, Carin
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  organization: Department of Immunology, Leiden University Medical Center, Leiden, the Netherlands
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  organization: Department of Immunology, Leiden University Medical Center, Leiden, the Netherlands
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  organization: Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands
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  surname: Haasnoot
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  givenname: Manon
  surname: Bos
  fullname: Bos, Manon
  organization: Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands
– sequence: 13
  givenname: Noel F.C.C.
  surname: de Miranda
  fullname: de Miranda, Noel F.C.C.
  organization: Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands
– sequence: 14
  givenname: Susana M.
  surname: Chuva de Sousa Lopes
  fullname: Chuva de Sousa Lopes, Susana M.
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  givenname: Marie-Louise P.
  surname: van der Hoorn
  fullname: van der Hoorn, Marie-Louise P.
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  givenname: Frits
  surname: Koning
  fullname: Koning, Frits
  organization: Department of Immunology, Leiden University Medical Center, Leiden, the Netherlands
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  givenname: Frans H.J.
  surname: Claas
  fullname: Claas, Frans H.J.
  organization: Department of Immunology, Leiden University Medical Center, Leiden, the Netherlands
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  givenname: Sebastiaan
  surname: Heidt
  fullname: Heidt, Sebastiaan
  organization: Department of Immunology, Leiden University Medical Center, Leiden, the Netherlands
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  givenname: Michael
  surname: Eikmans
  fullname: Eikmans, Michael
  email: m.eikmans@lumc.nl
  organization: Department of Immunology, Leiden University Medical Center, Leiden, the Netherlands
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Snippet Although the immunological complexity of the maternal-fetal interface is well appreciated, the actual interaction of maternal immune cells and fetal...
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SubjectTerms Biological sciences
Biological sciences research methodologies
Biotechnology
Immunology
Title Imaging mass cytometry reveals the prominent role of myeloid cells at the maternal-fetal interface
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